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MEDI-FIRST PLUS Ibuprofen - 47682-078-48 - (Ibuprofen)

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Drug Information of MEDI-FIRST PLUS Ibuprofen

Product NDC: 47682-078
Proprietary Name: MEDI-FIRST PLUS Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of MEDI-FIRST PLUS Ibuprofen

Product NDC: 47682-078
Labeler Name: Unifirst First Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA071333
Marketing Category: ANDA
Start Marketing Date: 20081230

Package Information of MEDI-FIRST PLUS Ibuprofen

Package NDC: 47682-078-48
Package Description: 125 PACKET in 1 BOX, UNIT-DOSE (47682-078-48) > 2 TABLET, FILM COATED in 1 PACKET

NDC Information of MEDI-FIRST PLUS Ibuprofen

NDC Code 47682-078-48
Proprietary Name MEDI-FIRST PLUS Ibuprofen
Package Description 125 PACKET in 1 BOX, UNIT-DOSE (47682-078-48) > 2 TABLET, FILM COATED in 1 PACKET
Product NDC 47682-078
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20081230
Marketing Category Name ANDA
Labeler Name Unifirst First Aid Corporation
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of MEDI-FIRST PLUS Ibuprofen


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